Search
for
Sort by
Research 721–750 of 1000+
- Common hair disorders.
- Itchy scalp with scale
- Philological Obfuscation
- TOC
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- Human tissue kallikreins as promiscuous modulators of homeostatic skin barrier functions
- Calcitriol-Resistant Rickets With Alopecia
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- A Clinical Study of Androgenetic Alopecia (V)
- Pseudallescheria boydii infection associated with IgG4-related disease
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Large Language Model versus Clinician Written Summaries of Research Papers
- 455 Beyond Immunity: TEC and JAK3 Kinase Activation in Melanocytes Drives Inflammation in Vitiligo
- Investigation of ROP GTPase Activity and Cytoskeleton Dynamics During Tip Growth in Root Hairs and Pollen Tubes
- Post SARS-CoV-2 vaccination effluvium
- Arecaceae
- Book reviews
- A child with generalized hypertrichosis due to secondary topical minoxidil exposure
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Hair follicle-specific keratins and their diseases
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Update on detection, morphology and fragility in pili annulati in three kindreds
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Formononetin: A Pathway to Protect Neurons
- Calcitriol-resistant rickets with alopecia
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report